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Namic H74904487202

by Medline Industries, Inc.

Namic H74904487202 is a Class II device made by Medline Industries, Inc., listed in FDA GUDID since 24 Feb 2022 (UDI-DI 10193489078022), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10193489078022 UDI-DI Date24 Feb 2022ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Namic
Generic name
Torque manipulation device
Model / Ref / Catalog
H74904487202
Primary DI / UDI-DI
10193489078022
FDA product code
DQX
GMDN term
Torque manipulation device
Device class
Class II
Regulation number
870.1330
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code DQX (Wire, guide, catheter).

Other devices from Medline Industries, Inc.

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Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)